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1.
Iron-rich concretions are frequently found around plant roots in Tagus estuary (Portugal) where radial delivery of O2 takes place. Salt marsh sediments exhibit cracks that are an additional feature to introduce O2 and other solutes in the upper sediments. Metal concentrations in salt marsh sediments are clearly above the background levels reflecting the anthropogenic sources from a large city with 2.5 million inhabitants, and several industrial centres. In order to evaluate how both oxidised structures influences the redistribution of redox sensitive elements in salt marsh sediments, concretions were collected from roots of Halimione portucaloides below the oxygenated zone. These tubular cylindrical structures were analysed for Fe, Al, Mn, As, and P along 1-cm radial transect in a millimetre scale from the inner part to the adjacent anoxic sediment. In addition, oxidised cracks were analysed for the same spatial resolution, from the sediment–water interface to anoxic layers (2-cm transept). The parallelism between Fe, As, and P concentrations at this microscale is the most noticeable aspect. Iron and As presented very high concentrations in the 4-mm concretions (3.4 mmol g−1 and 3.1 μmol g−1, respectively) and decreased sharply to the host sediment. Oxygen released from roots oxidise the solid sulphides, and the reduced Fe and As are transported towards the root by both diffusion and pore water flow associated with the root water uptake. Subsequently, Fe(III) precipitates and As is retained by sorption and/or coprecipitation. These elements are also enriched in the first 2-mm of oxidised cracks, but in lower concentrations (50% and 30%, respectively). Manganese concentrations in concretions were low (11.8 μmol g−1), indicating that Fe dominates the sediment chemistry. Phosphorus and iron concentrations in the ascorbate fraction were higher in the oxidising surfaces of concretions (10.7 μmol g−1 and 1.6 mmol g−1, respectively) and of cracks (5.1 μmol g−1 and 0.47 mmol g−1). The parallelism of Fe and As distributions includes not only their similar redox chemistries, but also that to phosphate, including control by coprecipitation of the host iron phases. The mechanisms involved in the mobilisation of As and P are however different, whereas As comes from the oxidation of iron sulphides; dissolved P derives from reduction of ferri-hydroxide phases.  相似文献   

2.
Environmental influences (temperature and oxygenation) on cod metabolism and their impact on the ecology of this species were investigated. Limiting oxygen concentration curves (O2 level ranging between 15 and 100% air saturation) were established at 2, 5 and 10°C. The standard metabolic rate (SMR), the maximum metabolic rate and the metabolic scope were then modelled as functions of temperature and/or oxygen saturation. The mean SMR at 2, 5 and 10°C were 19.8±4.9, 30.8±6.1 and 54.3±4.1 mg O2 h−1 kg−1, respectively. Between 2 and 5°C, the active metabolic rate of cod almost doubled from 65 to 120 mg O2 h−1 kg−1, to reach 177 mg O2 h−1 kg−1 at 10°C. In terms of metabolic scope (MS), the temperature rise from 2 to 5°C resulted in a two-fold increase from 45 to 89 mg O2 h−1 kg−1, with MS reaching 123 mg O2 h−1 kg−1 at 10°C. Our proposed model describing the impact of temperature and oxygen level provides new insight into the energetic interactions which govern the relationship between Atlantic cod and its environment. We re-examined published experimental and field studies from the angle of the regulation of metabolic power. We suggest that, when faced with heterogeneous or unstable hydrological conditions, cod tend to behaviourally maximise their metabolic scope. Through this adaptive response, fish reduce energy budgeting conflicts and presumably increase the probability of routinely operating away from lethal boundaries.  相似文献   

3.
The U-Tapao Canal is the main source of freshwater draining into the outer part of Songkhla Lake, which is the most important estuarine lagoon in Thailand. Songkhla Lake is located in southern Thailand between latitudes 7°08' and 7°50' N and longitudes 100°07' and 100°37' E. Acetic acid (HOAc)-soluble Cu, Fe, Mn, Pb, and Zn and the total concentration of these metals along with Al concentration, organic carbon, carbonate, sand, silt, and clay contents were determined in 4 sediment cores obtained at selected intervals from the mouth of the canal to 12 km upstream. Readily oxidizable organic matter in the cores varies from 1.52% to 7.30% and is generally found to decrease seaward. Total concentrations of Al (61.7–99.0 g kg−1; 2.29–3.67 mol kg−1), Cu (12.4–28.2 mg kg−1; 195–444 μmol kg−1), Fe (25.2–42.0 g kg−1; 451–752 mmol kg−1), Mn (0.22–0.49 g kg−1; 4.0–8.9 mmol kg−1), Pb (16.7–43.1 mg kg−1; 80.6–208 μmol kg−1), and Zn (48.6–122.7 mg kg−1; 0.74–1.88 mmol kg−1) vary to a certain extent vertically and seaward in the U-Tapao Canal core sediments. These concentrations are at or near natural levels and show no indication of anthropogenic contamination.Overall, the data show that total metal concentrations in the surface and near surface core sediments are enriched in varying degrees relative to Al in the order of Zn>Mn>Pb>Fe>Cu. Chemical partitioning shows that the enrichment in the surface and near surface sediments is related to the relatively high proportion of the total metal concentrations (Mn>Zn>Fe>Cu>Pb) that occur in the acetic acid-soluble (nondetrital) fraction, and they generally decrease with depth. Nondetrital Cu, Pb, and Zn likely derive from those metals held in ion exchange positions, certain carbonates, and from easily soluble amorphous compounds of Mn and perhaps those of Fe. Diagenetic processes involving Mn and to a lesser extent, Fe compounds, as well as the vertical changes in the oxidizing/reducing boundaries, appear to be the most important factors controlling the behavior of the metals in these cores. Organic matter and the aluminosilicate minerals, however, appear to be less important carriers of the metals studied.  相似文献   

4.
As part of a study of estuarine selenium cycling, we measured the concentration, chemical form (speciation), and distribution of particulate selenium under various river flow conditions in the North San Francisco Bay (from the Golden Gate to the Sacramento and San Joaquin Rivers). We also conducted laboratory studies on the accumulation of selenium by phytoplankton, the critical first step in the transformation of dissolved to particulate selenium. Total particulate selenium concentration in the North SF Bay was relatively constant between high and low flow periods, ranging spatially from 0.05 to 0.35 nmol l−1 and comprising between 5 and 12% of the total water column selenium inventory. Mean concentrations were generally highest in the Carquinez Strait–Suisun Bay region (salinity 0–17) and lowest in Central Bay. However, selenium content of suspended particles varied with river flow, with higher content during low flow (9.76 ± 4.17 nmol g−1; mean ± sd; n = 67) compared to high flow (7.10 ± 4.24 nmol g−1; n = 39). Speciation analyses showed that most particulate selenium is organic selenide (45 ± 27%), with a smaller proportion (typically <30%) of adsorbed selenite + selenate and a varying proportion (35 ± 28%) of elemental selenium. Based on the amount of elemental selenium in the seston (total suspended material), we calculate that resuspension of estuarine sediments could contribute 29–100% of particulate selenium in the water column. While selenium content of SF Bay seston (>0.4 μm) is relatively unenriched compared to phytoplankton (13.6–155 nmol g−1 dry weight) on a mass basis, when normalized to carbon or nitrogen, seston contains a similar selenium concentration to SF Bay sediments or phytoplankton cultures. SF Bay seston is thus comprised of selenium-rich phytoplankton and phyto-detritus, but also inorganic clay mineral particles that effectively “dilute” total particulate selenium. Selenium concentrations in algal cultures (11 species) exposed to 90 nmol l−1 selenite show relatively large differences in selenium accumulation, with the diatoms, chlorophytes and cryptophytes generally having lower selenium cell content (3.8 ± 2.7 × 10−9 nmol selenium cell−1) compared to the dinoflagellates (193 ± 73 × 10−9 nmol selenium cell−1). Because phytoplankton are such a rich (but variable) source of selenium, their dynamics could have a profound effect on the particulate selenium inventory in the North SF Bay.  相似文献   

5.
The formation of ferromanganese concretions on continental shelves is a widespread recent biogeochemical process, which is particularly intense in the Baltic Sea. The proposed new technique for dating ferromanganese concretions is based on the equilibrium 210Pb, which is produced immediately within them due to the decay of 226Ra, which is intensely sorbed by concretions from the seawater. This method is principally different from the traditional dating of bottom sediments using nonequilibrium 210Pb, which represents a decay product of atmospheric Ra. A mathematical tool for the calculation of the concretion ages is proposed. The latter is used for calculating the ages and growth rates of ferromanganese concretions belonging to two morphological varieties. The age and average growth rates of spheroidal concretions are estimated to be 670–850 years and 0.014 mm/year, respectively. The central part of a pancake-shaped concretion is dated back to 2500–3800 years, and its calculated respective horizontal and vertical growth rates are approximately 0.028 and 0.004 mm/year.  相似文献   

6.
Few data on dissolved trace metals in rivers and estuaries are presently available. This paper is an attempt to provide additional data on dissolved concentrations obtained in polluted and so-called unpolluted river estuarine systems. Data for two major French rivers (Gironde, Rhône) have been compared with the Chinese Yellow River (Huanghe) and Yangtze River (Changjiang). Dissolved Cd concentrations have been measured by differential pulse anodic stripping voltammetry. Average concentrations range from 15 ng kg−1 to 50 ng kg−1 (0.13–0.45 nmol kg−1) in the French rivers and are below 4 ng kg−1 (0.040 nmol kg−1) in the Chinese rivers.In all the estuaries studied the dissolved Cd concentrations depict a systematic bulge in the mixing zone which is attributed largely to remobilization processes from particulate matter when the chlorinity increases. Other parameters that may also play a significant role for remobilization are discussed. The processes concerned lead us to reassess the net Cd river input to the oceans, and this should be taken into account for a more precise evaluation of the residence time of oceanic Cd.  相似文献   

7.
Concentrations of Se in the pore-water and in the solid phase, and the concentrations of other diagenetic constituents (Fe, Mn, phosphate, ammonium and I) in pore-water, were determined in a sediment core from a 350-m deep station in the lower St. Lawrence Estuary. The concentration of dissolved Se in pore-water was 2.1 nmol kg−1 at the surface of the core, increasing to a maximum of 7.6 nmol kg−1 at a depth of 12 cm, and thereafter decreasing gradually with depth. This profile is similar to the profiles of Fe and phosphate, whose concentration maxima occur around 10 cm. The concentration of total sedimentary Se remained almost constant with depth (≈ 0.75 mg kg−1); however, a significant enrichment of oxalate-leachable Se was observed in the top 2 cm. The sedimentary cycling of Se appears to be closely related to that of Fe: adsorption of Se onto Fe oxyhydroxide at or near the sediment-water interface, release of the adsorbed Se by the reduction of Fe oxyhydroxide, and removal by formation of ferroselite (FeSe2) at depth. The pore-water flux of Se was estimated by two different methods, firstly from the pore-water gradient, and secondly by applying a box model to the oxalate-leachable solid-phase Se data. The methods agree well both giving values for the flux of 0.11 nmol cm−2 year−1. This agreement suggests that the loss of labile Se in the sediment is balanced by the upward flux of dissolved Se.  相似文献   

8.
The distributions of the trace metals iron (Fe), copper (Cu) and cadmium (Cd) along with hydrological parameters (salinity, temperature and reactive phosphate) across the New Zealand continental shelf near Otago Peninsula have been studied. This is a region in which the Subtropical Convergence (STC), a major oceanic front separating subtropical and subantarctic waters, is uniquely located close to land, permitting an examination of the influence of terrestrial sources of Fe and Cu on oceanic waters containing excess micronutrients. Acid-soluble (110 nmol kg−1) and dissolved (6.3 nmol kg−1) Fe concentrations were highest over the central shelf, and decreased rapidly across the mixing zone of the STC to about 5 nmol kg−1 for both forms. The distribution of acid-soluble and dissolved Cu were similar to their counterparts for Fe. Depth-concentration profiles for acid-soluble Fe and Cu suggest resuspension of shelf sediments is the main source. The ratio of oxine-labile to acid-soluble Fe varied from 0.03 to 0.26, with the highest values found in the near surface waters. Oxine-labile Fe and Cu also decreased in concentration in a seawards direction, and with depth, indicating the influence of near surface processes on the reactivity of these elements. Cd concentrations across the continental shelf were very low (<200 pmol kg−1) and exhibited no clear spatial trend and no correlation with phosphate. Comparison of the Cd/P ratio across the shelf indicated that the waters in this region were strongly depleted in Cd relative to P. Phosphate concentrations were lowest in neritic water and increased in the seawards direction because of mixing with nutrient-rich Subantarctic Surface Water.  相似文献   

9.
In September 1993 (M26) and June/July 1996 (M36), a total of 239 surface samples (7 m depth) were collected on two transects across the open Atlantic Ocean (224 samples) and northwest European shelf edge area. We present an overview of the horizontal variability of dissolved Cd, Co, Zn, and Pb in between the northwest and northeast Atlantic Ocean in relation to salinity and the nutrients. Our data show a preferential incorporation of Cd relative to P in the particulate material of the surface ocean when related to previously published parallel measurements on suspended particulate matter from the same cruise. There is a good agreement with results recently estimated from a model by Elderfield and Rickaby (Nature 405 (2000) 305), who predict for the North Atlantic Ocean a best fit for αCd/P=[Cd/P]POM/[Cd/P]SW of 2.5, whereas the approach of our transect shows a αCd/P value of 2.6. The Co concentrations of our transects varied from <5 to 131 pmol kg−1, with the lowest values in the subtropical gyre. There were pronounced elevations in the low-salinity ranges of the northwest Atlantic and towards the European shelf. The Co data are decoupled from the Mn distribution and support the hypothesis of marginal inputs as the dominant source. Zinc varied from a minimum of <0.07 nmol kg−1 to a maximum of 1.2 and 4.8 nmol kg−1 in regions influenced by Labrador shelf or European coastal waters, respectively. In subtropical and northeast Atlantic waters, the average Zn concentration was 0.16 nmol kg−1. Zinc concentrations at nearly three quarters of the stations between 40°N and 60°N were <0.1 nmol kg−1. This suggests that biological factors control Zn concentrations in large areas of the North Atlantic surface waters. The Pb data indicated that significant differences in concentration between the northwest and northeast Atlantic surface waters presently (1996) do not exist for this metal. The transects in 1993 and 1996 exhibited Pb concentrations in the northeast Atlantic surface waters of 30 to 40 pmol kg−1, about a fifth to a quarter of the concentrations observed in 1981. This decline is supported by our particle flux measurements in deep waters of the same region.  相似文献   

10.
Using the “Eikonal Approach” (Henyey et al., 1986), we estimate energy dissipation rates in the three-dimensional Garrett-Munk internal wave field. The total energy dissipation rate within the undisturbed GM internal wave field is found to be 4.34 × 10−9 W kg−1. This corresponds to a diapycnal diffusivity of about 0.3 × 10−4 m2s−1, which is less than the value 10−4 m2s−1 required to sustain the global ocean overturning circulation. Only when the high vertical wavenumber, near-inertial current shear is enhanced can diapycnal diffusivity reach ∼10−4 m2s−1. It follows that the energy supplied at low vertical wavenumbers and low frequencies is efficiently transferred to high vertical wavenumbers and near-inertial frequencies in the mixing hotspots in the real ocean.  相似文献   

11.
Common dab were fed a casein based diet containing copper at a concentration of 1·4 mg copper kg−1 (dry weight) or a similar diet supplemented with 200 mg copper kg−1. Fish were sampled after 10 weeks and 20 weeks and hepatic and renal copper, zinc and metallothionein concentrations were measured. All hepatic cytosolic copper in test and control fish co-eluted from Sephadex G-75 with metallothionein, as did some of the cytosolic zinc. After 20 weeks there was three times as much of this metallothionein-bound copper in the livers of the test fish compared to the control fish, although metallothionein concentration was little elevated. On the basis of these results it is proposed that cytosolic liver copper concentration or heat stable liver copper concentration can be used as an indication of excess dietary copper in the dab Limanda limanda.  相似文献   

12.
Fatty acids and hydrocarbons of sedimenting particles were investigated in the northeastern Adriatic Sea from November 1988 to December 1989. Particles were collected at approximately monthly intervals, using sediment traps deployed at 30 m depth (2 m above bottom). Seasonal changes in sedimentation of particulate matter were very pronounced. Hydrocarbon fluxes and concentrations were found to vary significantly depending on the season. They averaged 2.69 ± 1.44 mg m−2 day−1 and 232.4 ± 90.93 μg g−1 in winter, respectively. In late spring-early summer the corresponding values amounted to 0.045 ± 0.015 mg m−2 day−1 and 13.72 ± 5.56 μg g−1, and they increased towards autumn, when mean values of 0.517 ± 0.228 mg m−2 day−1 and 98.86 ± 48.72 μg g−1 were obtained. In contrast, fatty acid fluxes and concentrations were low during winter (0.26 ± 0.08 mg m−2 day−1 and 21.95 ± 3.35 μg g−1), increased slightly towards the summer (0.48 ± 0.12 mg m−2 day−1 and 139.9 ± 44.6 μ g−1) and reached maximum rate and concentration in autumn, when average values were 1.98 ± 1.30 mg m2 day−1 and 489.1 ± 186.7 μg g−1, respectively. The differences in composition, concentrations and fluxes of the fatty acids and hydrocarbons were related to the sources of sedimenting material, reflecting the influence of resuspension of bottom sediments during winter and the appearance of mucus aggregates during summer and their subsequent deposition in autumn.  相似文献   

13.
Climatological variability of picophytoplankton populations that consisted of >64% of total chlorophyll a concentrations was investigated in the equatorial Pacific. Flow cytometric analysis was conducted along the equator between 145°E and 160°W during three cruises in November–December 1999, January 2001, and January–February 2002. Those cruises were covering the La Niña (1999, 2001) and the pre-El Niño (2002) periods. According to the sea surface temperature (SST) and nitrate concentrations in the surface water, three regions were distinguished spatially, viz., the warm-water region with >28 °C SST and nitrate depletion (<0.1 μmol kg−1), the upwelling region with <28 °C SST and high nitrate (>4 μmol kg−1) water, and the in-between frontal zone with low nitrate (0.1–4 μmol kg−1). Picophytoplankton identified as the groups of Prochlorococcus, Synechococcus and picoeukaryotes showed a distinct spatial heterogeneity in abundance corresponding to the watermass distribution. Prochlorococcus was most abundant in the warm-water region, especially in the nitrate-depleted water with >150×103 cells ml−1, Synechococcus in the frontal zone with >15×103 cells ml−1, and picoeukaryotes in the upwelling region with >8×103 cells ml−1. The warm-water region extended eastward with eastward shift of the frontal zone and the upwelling region during the pre-El Niño period. On the contrary, these regions distributed westward during the La Niña period. These climatological fluctuations of the watermass significantly influenced the distribution of picophytoplankton populations. The most abundant area of Prochlorococcus and Synechococcus extended eastward and picoeukaryotes developed westward during the pre-El Niño period. The spatial heterogeneity of each picophytoplankton group is discussed here in association with spatial variations in nitrate supply, ambient ammonium concentration, and light field.  相似文献   

14.
Determinations of Cu, Co, Ni and Cd were carried out on 39 samples of surface seawaters from the Ligurian Sea, nearshore and offshore, between the Isola Capraia and Imperia. The concentrations of trace elements have been established employing the analytical method suggested by Le Meur and Courtot-Coupez (1973), by means of concentration of the sample by chelating resin, solvent extraction of the eluate and then by quantitative determination by AAS. The results obtained with this technique probably refer to ionic forms of the elements only. The Co concentration was lower than 0.15 μg 1−1 in 32 samples, with an average of 0.49 μg 1−1 for the others. For Cd, the greater number of samples had a content lower than 0.05 μg 1−1. For the others the mean concentration was 0.13 μg 1−1. The Ni had a mean concentration of 0.93 μg 1−1 and the average Cu content was 1.43 μg 1−1. Our data are in agreement with the values published by authors who have employed the same analytical technique. We observed that the offshore samples present a concentration lower than that in the nearshore samples.  相似文献   

15.
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16.
Copper concentrations have been measured in more than 200 samples collected from an Alaskan fjord and continental shelf and slope regions in the northwestern Gulf of Alaska. Concentrations were lowest (2·1 nmol kg−1) at depths of 400–1000 m in the continental slope waters of the Gulf of Alaska. Copper increased systematically with decreasing salinities shoreward to concentrations >30 nmol kg−1 in fjord surface waters during summer months of high freshwater runoff. Copper concentrations increased with depth at an inner fjord station where deep basin waters have restricted circulation, and these data together with surface (<5 cm) pore water copper concentrations (mean=122 nmol kg−1) about an order of magnitude higher than bottom water copper concentrations are indicative of a flux of copper across the sediment-seawater interface. This latter was estimated at 32±12 nmol cm−2 annually, and represented less than 20% of the annual input to fjord surface water (228–411 nmol cm−2) added during summer months. Mass balances in bottom waters indicate a vigorous recycling of copper with a residence time estimated at 21±11 days. Most copper that is remobilized in surface sediments is returned to bottom waters and little (3%) is removed by subsequent diagenetic reaction in the buried sediments. However, an estimate of copper accumulating in anoxic fjord sediments was comparable with copper added to fjord surface waters suggesting that input-removal reactions rather than internal cycling controls copper geochemistry in this estuary.  相似文献   

17.
Two toxic polypeptides BTTX I and BTTX II were isolated from the sea anemone Bolocera tuediae. Toxin isolation was achieved by alcoholic extraction of the homogenized tentacles and filaments, batchwise adsorption onto ion-exchangers (QAE-Sephadex A25, CM-Cellulose, Se-Cellulose, Sp-Sephadex C25), gel filtration on Sephadex G50 and G25 and ion-exchange chromatography on SP-Sephadex C25 and QAE-Sephadex A25. The toxins were tested on the shore crab Carcinus maenas by intramuscular injection. LD100 for BTTX I is 500 μg kg−1 C. maenas, whereas the BTTX II it is 40 μg kg−1. The molecular weights of both toxins are estimated to be 5000 Dalton.  相似文献   

18.
Macroalgae biomass and concentrations of nitrogen, phosphorus and chlorophyll a were determined weekly or biweekly in water and sediments, during the spring-summer of 1985 in a hypertrophic area of the lagoon of Venice. Remarkable biomass production (up to 286 g m−2 day−1, wet weight), was interrupted during three periods of anoxia, when macroalgal decomposition (rate: up to 1000 g m−2 day−1) released extraordinary amounts of nutrients. Depending on the macroalgae distribution in the water column, the nutrients released in water varied from 3·3 to 19·1 μg-at litre−1 for total inorganic nitrogen and from 1·8 to 2·7 μg-at litre−1 for reactive phosphorus. Most nutrients, however, accumulated in the surficial sediment (up to 0·640 and to 3·06 mg g−1 for P and N respectively) redoubling the amounts already stored under aerobic conditions, Phytoplankton, systematically below 5 mg m−3 as Chl. a, sharply increased up to 100 mg m−3 only after the release of nutrients in water by anaerobic macroalgal decomposition. During the algal growth periods, the N:P atomic ratio in water decreased to 0·7, suggesting that nitrogen is a growth-limiting factor. This ratio for surficial sediment was between 6·6 and 13·1, similar to that of macroalgae (8·6–12·0).  相似文献   

19.
The vertical flux of particulate matter at 330 m depth in San Lázaro Basin off southern Baja California ranged from 63 to 587 mg m−2 d−1 between August and November 1996. Organic carbon contents were between 5.6 and 14.8%, yielding flux rates of 9–40 mgC m−2 d−1. In December 1997 and January 1998, at the height of the strong El Niño event, the respective fluxes (47–202 mg m−2 d−1 and 3–8 mgC m−2 d−1) were comparable. The February–June 1998 records, however, revealed sharply reduced mass (1–6 mg m−2 d−1) and organic carbon (0.2–0.8 mgC m−2 d−1) fluxes. The organics collected in 1996 were predominantly autochthonous (δ13C=−22‰; C/N=8). The variations in δ15N (8.3–11.0‰) suggest an alternation of new and regenerated production, possibly associated with fluctuations in the intensity of deep mixing during that autumn. The relatively high organic matter fluxes in December 1997 appear to be associated with regenerated production. The average composition from February to June 1998 (δ13C=−23.6‰; 15N=11.7‰; C/N=10.5) indicates degraded material of marine origin. The maximum δ15N value found (14‰) suggests that deeper, denitrified waters were brought to the surface and possibly advected laterally. Regime changes in the waters of the basin occur at 6–10 week intervals, evidenced by concurrent shifts in most of the measured parameters, including fecal pellet types and metal chemistry. The marine snow-dominated detritus collected showed a shift from a mixed diatom-rich-radiolarian-coccolith assemblage in late 1996 to a coccolith-dominated assemblage, including the contents of fecal pellets, during the 1997–1998 El-Niño period. T–S profiles, plankton analysis and chlorophyll contents of the upper water column indicated that the strong phytoplankton bloom, normally associated with seasonal upwelling along the Pacific coast of Baja, did not occur during the spring of 1998. The persistence of oligotrophic conditions during the 1997–1998 El Niño event favored the dominance of nanoplankton and reduced the vertical flux of particles.  相似文献   

20.
An automated coulometric titration system based on that described by Johnson, Sieburth, Williams and Brandstrom (1987, Mar. Chem., 21: 117–133) has been evolved for the accurate and continual measurement of total dissolved inorganic carbon (TCO2). The instrument achieves an analytical precision (1 SD) of ±0.5–1.0 μmol kg−1 (0.025–0.05%). The accuracy of the system has been examined by a limited comparison with other coulometric-based titrators and with a manometric-based system; agreement was to 1 μmol kg−1. The capability for automatic continual analysis allows surface mapping of TCO2; a sample rate of 10 analyses h−1 gives a mapping resolution of 1–2 km. Provision for frequent standardization with a liquid substandard has been included in the development. The ability to achieve high-density analyses while maintaining interlaboratory consistency and standardization constitutes a vital contribution to surveys of ocean carbon chemistry (e.g. Joint Global Ocean Flux Study, World Ocean Circulation Experiment).  相似文献   

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